HGVS | Genome Assembly |
---|---|
NC_000005.10:g.60491901T= , CM000667.2:g.60491901T= | GRCh38 |
NC_000005.9:g.59787728T= , CM000667.1:g.59787728T= | GRCh37 |
NC_000005.8:g.59823485T= | NCBI36 |
NG_027957.1:g.1198A= | |
NG_027957.2:g.37429A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506510.6:n.70+30150A= (PDE4D) | ||
NR_024617.1:n.711+3478T= (PART1) | ||
NR_028509.1:n.492+3478T= (PART1) | ||
XM_011543472.1:c.-90+30150A= (PDE4D) | XP_011541774.1:n.-90+30150A= | |
NM_001364599.1:c.-90+4238A= (PDE4D) | NP_001351528.1:n.-90+4238A= | |
XM_024446110.1:c.-90+30150A= (PDE4D) | XP_024301878.1:n.-90+30150A= | |
XM_024446112.1:c.-90+30150A= (PDE4D) | XP_024301880.1:n.-90+30150A= |